JPS6178759A - 置換カルボジイミド及びその製造方法並びに殺虫・殺ダニ組成物 - Google Patents
置換カルボジイミド及びその製造方法並びに殺虫・殺ダニ組成物Info
- Publication number
- JPS6178759A JPS6178759A JP60207723A JP20772385A JPS6178759A JP S6178759 A JPS6178759 A JP S6178759A JP 60207723 A JP60207723 A JP 60207723A JP 20772385 A JP20772385 A JP 20772385A JP S6178759 A JPS6178759 A JP S6178759A
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- alkyl group
- substituted
- atom
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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- 238000004519 manufacturing process Methods 0.000 title claims description 3
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- 150000001875 compounds Chemical class 0.000 claims description 86
- 125000000217 alkyl group Chemical group 0.000 claims description 68
- 125000005843 halogen group Chemical group 0.000 claims description 55
- 239000004480 active ingredient Substances 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 34
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 29
- 125000003545 alkoxy group Chemical group 0.000 claims description 22
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 22
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 22
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 21
- 125000005554 pyridyloxy group Chemical group 0.000 claims description 21
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 20
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
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- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- 125000001188 haloalkyl group Chemical group 0.000 claims description 10
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- 125000003367 polycyclic group Chemical group 0.000 claims description 5
- 241001465754 Metazoa Species 0.000 claims description 4
- 150000001721 carbon Chemical group 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
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- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 2
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- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
- 125000006313 (C5-C8) alkyl group Chemical group 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
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- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 4
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
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- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 241000257303 Hymenoptera Species 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
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- 125000003827 glycol group Chemical group 0.000 description 1
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- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
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- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
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- 239000003921 oil Substances 0.000 description 1
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- 239000011541 reaction mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
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- 235000020354 squash Nutrition 0.000 description 1
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- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
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- 238000003756 stirring Methods 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
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- 239000012085 test solution Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
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- 239000002966 varnish Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
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- 150000003738 xylenes Chemical class 0.000 description 1
Landscapes
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH447984 | 1984-09-19 | ||
CH4479/84-9 | 1984-09-19 | ||
CH3526/85-5 | 1985-08-15 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6178759A true JPS6178759A (ja) | 1986-04-22 |
JPH0417945B2 JPH0417945B2 (enrdf_load_stackoverflow) | 1992-03-26 |
Family
ID=4276862
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60207723A Granted JPS6178759A (ja) | 1984-09-19 | 1985-09-19 | 置換カルボジイミド及びその製造方法並びに殺虫・殺ダニ組成物 |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPS6178759A (enrdf_load_stackoverflow) |
ZA (1) | ZA857153B (enrdf_load_stackoverflow) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5069226A (enrdf_load_stackoverflow) * | 1973-10-23 | 1975-06-10 | ||
JPS5077328A (enrdf_load_stackoverflow) * | 1973-11-09 | 1975-06-24 | ||
JPS5266623A (en) * | 1975-11-27 | 1977-06-02 | Bayer Ag | Ectoparasite killing composition containing diphenylcarboxymid and ammonia salt |
-
1985
- 1985-09-18 ZA ZA857153A patent/ZA857153B/xx unknown
- 1985-09-19 JP JP60207723A patent/JPS6178759A/ja active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5069226A (enrdf_load_stackoverflow) * | 1973-10-23 | 1975-06-10 | ||
JPS5077328A (enrdf_load_stackoverflow) * | 1973-11-09 | 1975-06-24 | ||
JPS5266623A (en) * | 1975-11-27 | 1977-06-02 | Bayer Ag | Ectoparasite killing composition containing diphenylcarboxymid and ammonia salt |
Also Published As
Publication number | Publication date |
---|---|
JPH0417945B2 (enrdf_load_stackoverflow) | 1992-03-26 |
ZA857153B (en) | 1986-05-28 |
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